Dyschromatosis universalis hereditaria
A rare genetic pigmentation anomaly of the skin characterized by generalized irregularly shaped asymptomatic hyper- and hypopigmented macules distributed in a reticular pattern involving the trunk limbs and sometimes the face. The palms soles and mucosa are usually not affected. Systemic abnormalities have been rarely reported.
Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview.
Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http://www.orphadata.org. Data version December 2023
Newly diagnosed with
Dyschromatosis universalis hereditaria?
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Syndromes Without A Name (SWAN) Australia
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